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Published on: May 25, 2017
Vascular endothelial cell distribution and adhesion molecule expression in xanthoma
Masaaki Matsumoto1, Sawa Kunimitsu, Kana Wada
1Department of Dermatology, Kochi Medical School, Okohcho, Nankoku, Kochi, Japan. matsumo@kochu-u.ac.jp
Endothelial cells in xanthoma lesions express E-selectin, promoting macrophage migration. This contrasts with normal skin, where intercellular cell adhesion molecule-1 (ICAM-1) is more prevalent, influencing xanthoma development.
Area of Science:
- Dermatology
- Immunology
- Cell Biology
Background:
- Monocyte migration into the dermis is crucial for xanthoma initiation and progression.
- The role of vascular endothelial cells in monocyte migration during xanthoma is not well understood.
Purpose of the Study:
- To investigate the role of endothelial cells and their associated molecules in xanthoma pathogenesis.
- To compare endothelial cell markers in xanthoma lesions versus normal skin.
Main Methods:
- Immunohistochemical staining was performed on 20 xanthelasma and 6 tuberous xanthoma lesions.
- Analysis focused on the expression of von Willebrand factor, E-selectin, and intercellular cell adhesion molecule-1 (ICAM-1) on endothelial cells.
Main Results:
- Xanthoma lesions showed a 25-fold increase in von Willebrand factor-positive endothelial cells compared to normal skin.
- E-selectin-positive endothelial cells were threefold more prevalent in xanthoma lesions, while ICAM-1 expression decreased by 3.5-fold.
- A higher ratio of macrophages to endothelial cells (10:1) was observed in xanthoma lesions compared to normal skin (5:1).
Conclusions:
- Endothelial cells in xanthoma lesions proliferate and express E-selectin, not ICAM-1, in a macrophage-rich environment.
- This altered endothelial cell expression promotes further macrophage migration into xanthoma lesions.
- The findings highlight a shift in endothelial cell behavior that contributes to xanthoma progression.
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